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The effect of dapagliflozin on allograft function following kidney transplantation: A randomized controlled open-label study (ALL-FOR-ONE study)

The effect of dapagliflozin on allograft function following kidney transplantation: A randomized controlled open-label study (ALL-FOR-ONE study)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1051210190
Enrollment
130
Registered
2022-03-09
Start date
2022-03-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

kidney transplantation

Interventions

Dapagliflozin group: In addition to the standard treatment, dapagliflozin (10 mg orally once daily) will be started within 70 days of enrollment and continued until the end of treatment (104 weeks). N

Sponsors

Mizui Masayuki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All of the following criteria are met (1) Patients aged 20 years or older but less than 80 years (2) Patients with an eGFR of 30 mL/min/1.73 m2 or higher during the screening period (data within 3 months prior to enrollment are acceptable) (3) Patients who have undergone kidney transplantation for more than 1 year (4) Patients who have given written consent

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria will be excluded from this study. (1) Patients with a history of organ transplantation other than kidney (2) Patients on SGLT2 inhibitor (if the medication was terminated more than 6 months ago, it is acceptable) (3) Patients who are not expected to survive for more than 2 years after enrollment (4) Patients who have experienced rejection within 3 months (5) Women who plan to become pregnant within 3 years (6) Lactating women, pregnant women or patients who may be pregnant (7) Patients suffering from active infectious disease (8) Patients with a history of hypersensitivity to the components of dapagliflozin products. (9) Patients who are judged inappropriate by the principal investigator or sub-investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
eGFR slope (mL/min/1.73 m2/year)

Secondary

MeasureTime frame
(1) Change in eGFR Change in eGFR value at the end of observation (4 weeks after the end of treatment) relative to Baseline eGFR value (mL/min/1.73 m2) (2) Changes in urine protein/creatinine ratio, urine beta2-MG/creatinine ratio, and urine beta2-MG concentration (3) Changes in interstitial fibrosis and tubular atrophy in transplant kidney biopsy (4) Effect on (renal) anemia: changes in TSAT, ferritin, hemoglobin, and erythropoietin (5) Effect on bone mineral metabolism: changes in Ca, P, Mg, iPTH (6) Rate of new-onset of malignancy (7) Change in renal volume (calculated by CT) (8) Change in the transplant kidney prognostic score (iBox)

Contacts

Public ContactYohei Doi

The University of Osaka Hospital

ydoi@kid.med.osaka-u.ac.jp+81-6-6879-3857

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026